Romano A - Search Results

1

A further contribution to the delineation of epileptic phenotype in PACS2-related syndrome.

Terrone G, Marchese F, Vari MS, Severino M, Madia F, Amadori E, Del Giudice E, Romano A, Gennaro E, Zara F, Striano P. Terrone G, et al. Among authors: romano a. Seizure. 2020 Jul;79:53-55. doi: 10.1016/j.seizure.2020.05.001. Epub 2020 May 11. Seizure. 2020. PMID: 32416568 Free article. No abstract available.

2

EEG findings in West syndrome a follow-up of 20 patients.

Vacca G, de Falco FA, Natale S, del Giudice E, Romano A, Latte F, Bianchi L. Vacca G, et al. Among authors: romano a. Acta Neurol (Napoli). 1992 Aug-Dec;14(4-6):297-303. Acta Neurol (Napoli). 1992. PMID: 1338179

3

Upper gastrointestinal tract motility in children with progressive muscular dystrophy.

Staiano A, Del Giudice E, Romano A, Andreotti MR, Santoro L, Marsullo G, Rippa PG, Iovine A, Salvatore M. Staiano A, et al. Among authors: romano a. J Pediatr. 1992 Nov;121(5 Pt 1):720-4. doi: 10.1016/s0022-3476(05)81899-2. J Pediatr. 1992. PMID: 1432420

4

Familial white matter hypoplasia, agenesis of the corpus callosum, mental retardation and growth deficiency: a new distinctive syndrome.

Curatolo P, Cilio MR, Del Giudice E, Romano A, Gaggero R, Pessagno A. Curatolo P, et al. Among authors: romano a. Neuropediatrics. 1993 Apr;24(2):77-82. doi: 10.1055/s-2008-1071518. Neuropediatrics. 1993. PMID: 8327066

5

Gastrointestinal manifestations in children with cerebral palsy.

Del Giudice E, Staiano A, Capano G, Romano A, Florimonte L, Miele E, Ciarla C, Campanozzi A, Crisanti AF. Del Giudice E, et al. Among authors: romano a. Brain Dev. 1999 Jul;21(5):307-11. doi: 10.1016/s0387-7604(99)00025-x. Brain Dev. 1999. PMID: 10413017 Clinical Trial.

6

Short duration outpatient video electroencephalographic monitoring: the experience of a southern-Italian general pediatric department.

Del Giudice E, Crisanti AF, Romano A. Del Giudice E, et al. Among authors: romano a. Epileptic Disord. 2002 Sep;4(3):197-202. Epileptic Disord. 2002. PMID: 12446222 Free article.

7

Acute inflammatory demyelinating polyradiculoneuropathy associated with perforin-deficient familial haemophagocytic lymphohistiocytosis.

Del Giudice E, Savoldi G, Notarangelo LD, Di Benedetto L, Manganelli F, Bruzzese E, Romano A, Santoro L. Del Giudice E, et al. Among authors: romano a. Acta Paediatr. 2003;92(3):398-401. Acta Paediatr. 2003. PMID: 12725560

8

Mild Wolf-Hirschhorn phenotype and partial GH deficiency in a patient with a 4p terminal deletion.

Titomanlio L, Romano A, Conti A, Genesio R, Salerno M, De Brasi D, Nitsch L, Del Giudice E. Titomanlio L, et al. Among authors: romano a. Am J Med Genet A. 2004 Jun 1;127A(2):197-200. doi: 10.1002/ajmg.a.20667. Am J Med Genet A. 2004. PMID: 15108211

9

Cerebellar agenesis.

Titomanlio L, Romano A, Del Giudice E. Titomanlio L, et al. Among authors: romano a. Neurology. 2005 Mar 22;64(6):E21. doi: 10.1212/wnl.64.6.e21. Neurology. 2005. PMID: 15781801 No abstract available.

10

Partial cerebellar hypoplasia in a patient with Prader-Willi syndrome.

Titomanlio L, De Brasi D, Romano A, Genesio R, Diano AA, Del Giudice E. Titomanlio L, et al. Among authors: romano a. Acta Paediatr. 2006 Jul;95(7):861-3. doi: 10.1080/08035250500527307. Acta Paediatr. 2006. PMID: 16801186

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